Abstract
Noonan syndrome with multiple lentigines (NSML) is a rare RASopathy caused by pathogenic variants (PV) predominantly in PTPN11 gene. We report a 54‐year‐old male with apical hypertrophic cardiomyopathy, who was diagnosed with NSML due to his short stature, multiple lentigines, winged neck, pectus excavatum, and a heterozygous PV in PTPN11 c.836A > ¡G.
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CITATION STYLE
APA
Rivero‐García, P., Campuzano‐Estrada, I. del C., & Hernandez‐Felix, J. H. (2023). Hypertrophic cardiomyopathy in an adult patient with Noonan syndrome with multiple lentigines. Clinical Case Reports, 11(6). https://doi.org/10.1002/ccr3.7607
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